HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 5-(1,1-Dimethylethyl)-1H-indole-2-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | ethyl 5-tert-butyl-1H-indole-2-carboxylate | HCID 4714960 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(1,1-Dimethylethyl)-1H-indole-2-carboxylic acid | HCID 4642229 | 93% |
Reaction Steps
A solution of ethyl 5-tert-butylindole-2-carboxylate (3.0 g) and 1N sodium hydroxide solution into a mixed solvent of tetrahydrofuran (20 ml) and methanol (10 ml) was stirred at 40° C. for 5 hours. After removal of solvent, the resulting aqueous solution was made acidic with diluted hydrochloric acid. The resulting precipitates were collected by filtration and washed with water to give 5-tert-butylindole-2-carboxylic acid (2.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994378 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-a368667c31004cfebab55819c953ed57 |
| Source note | uspto-grants-1999_11 |